Document Detail


The pathogenesis of sepsis.
MedLine Citation:
PMID:  20887193     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Sepsis is a serious clinical condition that represents a patient's response to a severe infection and has a very high mortality rate. Normal immune and physiologic responses eradicate pathogens, and the pathophysiology of sepsis is due to the inappropriate regulation of these normal reactions. In an ideal scenario, the first pathogen contact with the inflammatory system should eliminate the microbe and quickly return the host to homeostasis. The septic response may accelerate due to continued activation of neutrophils and macrophages/monocytes. Upregulation of lymphocyte costimulatory molecules and rapid lymphocyte apoptosis, delayed apoptosis of neutrophils, and enhanced necrosis of cells/tissues also contribute to the pathogenesis of sepsis. The coagulation system is closely tied to the inflammatory response, with cross talk between the two systems driving the dysregulated response. Biomarkers may be used to help diagnose patients with sepsis, and they may also help to identify patients who would benefit from immunomodulatory therapies.
Authors:
Deborah J Stearns-Kurosawa; Marcin F Osuchowski; Catherine Valentine; Shinichiro Kurosawa; Daniel G Remick
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Annual review of pathology     Volume:  6     ISSN:  1553-4014     ISO Abbreviation:  Annu Rev Pathol     Publication Date:  2011  
Date Detail:
Created Date:  2011-01-25     Completed Date:  2011-04-25     Revised Date:  2012-03-14    
Medline Journal Info:
Nlm Unique ID:  101275111     Medline TA:  Annu Rev Pathol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  19-48     Citation Subset:  IM    
Affiliation:
Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Massachusetts 02218, USA. dstearns@bu.edu
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MeSH Terms
Descriptor/Qualifier:
Acute Disease
Biological Markers*
Blood Coagulation / immunology*
Critical Illness*
Female
Humans
Middle Aged
Sepsis / immunology*,  therapy*
Grant Support
ID/Acronym/Agency:
R01 GM082962-03/GM/NIGMS NIH HHS; R01 GM082962-04/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Biological Markers

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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